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au.\*:("TONIOLO D")

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PROCESSING OF RIBOSOMAL RNA IN A TEMPERATURE SENSITIVE MUTANT OF BHK CELLSTONIOLO D; BASILICO C.1976; BIOCHIM. BIOPHYS. ACTA; PAYS-BAS; DA. 1976; VOL. 425; NO 4; PP. 409-418; BIBL. 18 REF.Article

SV40-TRANSFORMED CELLS WITH TEMPERATURE-DEPENDENT SERUM REQUIREMENTSTONIOLO D; BASILICO C.1975; CELL; U.S.A.; DA. 1975; VOL. 4; NO 3; PP. 255-262; BIBL. 25REF.Article

COMPLEMENTATION OF A DEFECT IN THE PRODUCTION OF RIBOSOMAL RNA IN SOMATIC CELL HYBRIDSTONIOLO D; BASILICO C.1974; NATURE; G.B.; DA. 1974; VOL. 248; NO 5447; PP. 411-413; BIBL. 12REF.Article

FAST-NEUTRON TRANSMISSION THROUGH A POLARIZED HOLMIUM TARGETFASOLI U; GALEAZZI G; TONIOLO D et al.1973; LETTERE NUOVO CIMENTO; ITAL.; DA. 1973; VOL. 6; NO 13; PP. 485-490; BIBL. 8 REF.Serial Issue

NEUTRON-CARBON INTERACTION: TOTAL AND ELASTIC SCATTERING DIFFERENTIAL CROSS SECTIONS AND PHASE SHIFT ANALYSIS, 2.1 TO 4.7 MEVFASOLI U; METELLINI A; TONIOLO D et al.1973; NUCL. PHYS., A; NETHERL.; DA. 1973; VOL. 205; NO 2; PP. 305-320; BIBL. 26 REF.Serial Issue

CDNA SEQUENCES OF HUMAN GLUCOSE 6-PHOSPHATE DEHYDROGENASE CLONED IN PBR 322 = SEQUENCES D'ADNC DE LA GLUCOSE PHOSPHATE-6 DESHYDROGENASE HUMAINE CLONEES DANS PBR 322PERSICO MG; TONIOLO D; NOBILE C et al.1981; NATURE (LOND.); ISSN 0028-0836; GBR; DA. 1981; VOL. 294; NO 5843; PP. 778-780; BIBL. 33 REF.Article

SOLITON FISSION AND TUNNELLING IN ELECTRIC LINESBON P; MINELLI TA; PASCOLINI A et al.1982; LETT. NUOVO CIMENTO SOC. ITAL. FIS.; ISSN 0375-930X; ITA; DA. 1982; VOL. 35; NO 9; PP. 279-284; BIBL. 7 REF.Article

CpG islands of the X chromosome are gene associatedALCALAY, M; TONIOLO, D.Nucleic acids research. 1988, Vol 16, Num 20, pp 9527-9543, issn 0305-1048Article

REGULATION OF GLUCOSE 6-PHOSPHATE DEHYDROGENASE EXPRESSION IN CHO-HUMAN FIBROBLAST SOMATIC CELL HYBRIDSD'URSO M; MARENI C; TONIOLO D et al.1983; SOMATIC CELL GENETICS; ISSN 0098-0366; USA; DA. 1983; VOL. 9; NO 4; PP. 429-443; BIBL. 27 REF.Article

Stability of DNA methylation of X-chromosome genes during agingPAGANI, F; TONIOLO, D; VERGANI, C et al.Somatic cell and molecular genetics. 1990, Vol 16, Num 1, pp 79-84, issn 0740-7750Article

Selection and fine mapping of chromosome-specific cDNAs : Application to human chromosome 1MANCINI, M; SALA, C; RIVELLA, S et al.Genomics (San Diego, Calif.). 1996, Vol 38, Num 2, pp 149-154, issn 0888-7543Article

Ultrastructural abnormality of sarcolemmal nuclei in Emery-Dreifuss muscular dystrophy (EDMD)FIDZIANSKA, A; TONIOLO, D; HAUSMANOWA-PETRUSEWICZ, I et al.Journal of the neurological sciences. 1998, Vol 159, Num 1, pp 88-93, issn 0022-510XArticle

A housekeeping gene on the X chromosome encodes a protein similar to ubiquitinTONIOLO, D; PERSICO, M; ALCALAY, M et al.Proceedings of the National Academy of Sciences of the United States of America. 1988, Vol 85, Num 3, pp 851-855, issn 0027-8424Article

Expression of the G6PD locus on the human X chromosome is associated with demethylation of three CpG islands within 100 kb of DNATONIOLO, D; MARTINI, G; MIGEON, B. R et al.EMBO journal (Print). 1988, Vol 7, Num 2, pp 401-406, issn 0261-4189Article

The CpG island in the 5' region of the G6PD gene of man and mouseTONIOLO, D; FILIPPI, M; DONO, R et al.Gene (Amsterdam). 1991, Vol 102, Num 2, pp 197-203, issn 0378-1119Article

Partial purification and characterization of the Messenger RNA for human glucose-6-phosphate dehydrogenaseTONIOLO, D; PERSICO, M. G; BATTISTUZZI, G et al.Molecular biology & medicine. 1984, Vol 2, Num 2, pp 89-103, issn 0735-1313Article

Familial periventricular heterotopia: Missense and distal truncating mutations of the FLN1 geneMORO, F; CARROZZO, R; VEGGIOTTI, P et al.Neurology. 2002, Vol 58, Num 6, pp 916-921, issn 0028-3878Article

Identification of a novel X-linked gene responsible for Emery-Dreifuss muscular dystrophyBIONE, S; MAESTRINI, E; RIVELLA, S et al.Nature genetics. 1994, Vol 8, Num 4, pp 323-327, issn 1061-4036Article

Physical map of human Xq27-qter : localizing the region of the fragile X mutationPOUSTKA, A; DIETRICH, A; LANGENSTEIN, G et al.Proceedings of the National Academy of Sciences of the United States of America. 1991, Vol 88, Num 19, pp 8302-8306, issn 0027-8424Article

Two point mutations are responsible for G6PD polymorphism in SardiniaDE VITA, G; ALCALAY, M; SAMPIETRO, M et al.American journal of human genetics. 1989, Vol 44, Num 2, pp 233-240, issn 0002-9297Article

Selection and mapping of replication origins from a 500-kb region of the human X chromosome and their relationship to gene expressionRIVELLA, S; PALERMO, B; PELIZON, C et al.Genomics (San Diego, Calif.). 1999, Vol 62, Num 1, pp 11-20, issn 0888-7543Article

Safety profile of ofloxacin: the Italian date baseKOVERECH, A; PICARI, M; GRANATA, F et al.Infection. 1986, Vol 14, pp S335-S337, issn 0300-8126, suppl. 4Article

Tissue-specific levels of human glucose-6-phosphate dehydrogenase correlate with methylation of specific sites at the 3' end of the geneBATTISTUZZI, G; DURSO, M; TONIOLO, D et al.Proceedings of the National Academy of Sciences of the United States of America. 1985, Vol 82, Num 5, pp 1465-1469, issn 0027-8424Article

Duplications fo the X chromosome in males : evidence that most parts of the X chromosome can be active in two copiesSCHMIDT, M; DU SART, D; KALITSIS, P et al.Human genetics. 1991, Vol 86, Num 5, pp 519-521, issn 0340-6717Article

A novel X-linked gene, G4.5. is responsible for Barth syndromeBIONE, S; D'ADAMO, P; MAESTRINI, E et al.Nature genetics. 1996, Vol 12, Num 4, pp 385-389, issn 1061-4036Article

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